Imidazopyridyl compounds as aldosterone synthase inhibitors
Granted 3 Nov 2015 · 2 office actions
Current assignee: Merck Sharp & Dohme · originally Merck & Co., Inc.
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Inventors: D. Jonathan Bennett, Michael Lo, Jaiqiang Cai, Yusheng Xiong +10 · Examiner: Timothy R Rozof · AU 1625 · TC 1600
Life of the patent
4 dated eventsAbstract
This invention relates to imidazopyridyl compounds of the structural formula: I or their pharmaceutically acceptable salts, wherein the variable are defined herein. The inventive compounds selectively inhibit aldosterone synthase. This invention also provides for pharmaceutical compositions comprising the compounds of Formula I or their salts as well as potentially to methods for the treatment, amelioration or prevention of conditions that could be treated by inhibiting aldosterone synthase. [structure]
Claims
9 · 1 independent · depth 2Classifications
3 codes- A61K31/437
- C07D487/04
- C07D471/04
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2 priority documents›Priority documents — 2
| Type | Document | Date |
|---|---|---|
| provisional | US 61537910 | 22 Sep 2011 |
| related publication | US 20140235667 A1 | 21 Aug 2014 |
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